Pharmacological Properties of Sulfonamide Derivatives, New Inhibitors of Carbonic Anhydrase
Selective blocking of individual isoforms of carbonic anhydrase (CA) is now one of the main directions in the development of its inhibitors. The new 1,2,4-oxadiazole-containing sulfonamides B12 and B13 predominantly block CA II and CA IX. The study of acute toxicity of B12 and B13 showed their safet...
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| Vydané v: | Bulletin of experimental biology and medicine Ročník 175; číslo 2; s. 205 - 209 |
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| Hlavní autori: | , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
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01.06.2023
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| ISSN: | 0007-4888, 1573-8221, 1573-8221 |
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| Abstract | Selective blocking of individual isoforms of carbonic anhydrase (CA) is now one of the main directions in the development of its inhibitors. The new 1,2,4-oxadiazole-containing sulfonamides B12 and B13 predominantly block CA II and CA IX. The study of acute toxicity of B12 and B13 showed their safety. Substance B13 caused a relatively short-term, but rapid (within 30 min) decrease in the intraocular pressure in rabbits, which indicates the promise of its use for the emergency decrease in the intraocular pressure in medical practice. Analysis of the effects of sulfonamides on the functions of CNS showed that compound B12 probably exhibit tranquilizing activity; B13 is promising for the creation of drugs that have an antidepressant effect and at the same time increase the mental and physical performance. |
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| AbstractList | Selective blocking of individual isoforms of carbonic anhydrase (CA) is now one of the main directions in the development of its inhibitors. The new 1,2,4-oxadiazole-containing sulfonamides B12 and B13 predominantly block CA II and CA IX. The study of acute toxicity of B12 and B13 showed their safety. Substance B13 caused a relatively short-term, but rapid (within 30 min) decrease in the intraocular pressure in rabbits, which indicates the promise of its use for the emergency decrease in the intraocular pressure in medical practice. Analysis of the effects of sulfonamides on the functions of CNS showed that compound B12 probably exhibit tranquilizing activity; B13 is promising for the creation of drugs that have an antidepressant effect and at the same time increase the mental and physical performance.Selective blocking of individual isoforms of carbonic anhydrase (CA) is now one of the main directions in the development of its inhibitors. The new 1,2,4-oxadiazole-containing sulfonamides B12 and B13 predominantly block CA II and CA IX. The study of acute toxicity of B12 and B13 showed their safety. Substance B13 caused a relatively short-term, but rapid (within 30 min) decrease in the intraocular pressure in rabbits, which indicates the promise of its use for the emergency decrease in the intraocular pressure in medical practice. Analysis of the effects of sulfonamides on the functions of CNS showed that compound B12 probably exhibit tranquilizing activity; B13 is promising for the creation of drugs that have an antidepressant effect and at the same time increase the mental and physical performance. Selective blocking of individual isoforms of carbonic anhydrase (CA) is now one of the main directions in the development of its inhibitors. The new 1,2,4-oxadiazole-containing sulfonamides B12 and B13 predominantly block CA II and CA IX. The study of acute toxicity of B12 and B13 showed their safety. Substance B13 caused a relatively short-term, but rapid (within 30 min) decrease in the intraocular pressure in rabbits, which indicates the promise of its use for the emergency decrease in the intraocular pressure in medical practice. Analysis of the effects of sulfonamides on the functions of CNS showed that compound B12 probably exhibit tranquilizing activity; B13 is promising for the creation of drugs that have an antidepressant effect and at the same time increase the mental and physical performance. Selective blocking of individual isoforms of carbonic anhydrase (CA) is now one of the main directions in the development of its inhibitors. The new 1,2,4-oxadiazole-containing sulfonamides B12 and B13 predominantly block CA II and CA IX. The study of acute toxicity of B12 and B13 showed their safety. Substance B13 caused a relatively short-term, but rapid (within 30 min) decrease in the intraocular pressure in rabbits, which indicates the promise of its use for the emergency decrease in the intraocular pressure in medical practice. Analysis of the effects of sulfonamides on the functions of CNS showed that compound B12 probably exhibit tranquilizing activity; B13 is promising for the creation of drugs that have an antidepressant effect and at the same time increase the mental and physical performance. Key Words: carbonic anhydrases; carbonic anhydrase inhibitors; sulfonamides; intraocular pressure |
| Audience | Academic |
| Author | Korsakov, M. K. Tyushina, A. N. Volkhin, N. N. Shetnev, A. A. Fedorov, V. N. Vdovichenko, V. P. Khokhlov, A. L. |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37464193$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.3109/14756366.2015.1122001 10.18008/1816-5095-2020-4-676-682 10.1517/13543776.2012.649006 10.1080/13543776.2018.1519023 10.18008/1816-5095-2020-3S-542-549 10.1016/j.bioorg.2019.103557 10.1017/CBO9781139344319 10.1016/j.ejmech.2019.02.044 10.1124/jpet.110.167270 |
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| References | Ghorai S, Pulya S, Ghosh K, Panda P, Ghosh B, Gayen S. Structure-activity relationship of human carbonic anhydrase-II inhibitors: Detailed insight for future development as anti-glaucoma agents. Bioorg. Chem. 2020;95:103557. doi: https://doi.org/10.1016/j.bioorg.2019.103557 CartaFSupuranCTScozzafavaANovel therapies for glaucoma: a patent review 2007–2011Expert Opin. Ther. Pat.201222179881:CAS:528:DC%2BC38Xjs1Cqug%3D%3D10.1517/13543776.2012.64900622191414 SupuranCTApplications of carbonic anhydrases inhibitors in renal and central nervous system diseasesExpert Opin. Ther. Pat.201828107137211:CAS:528:DC%2BC1cXhs1Olt77I10.1080/13543776.2018.151902330175635 CianchiFVinciMCSupuranCTPeruzziBDe GiuliPFasolisGPerigliGPastorekovaSPapucciLPiniAMasiniEPuccettiLSelective inhibition of carbonic anhydrase IX decreases cell proliferation and induces ceramide-mediated apoptosis in human cancer cellsJ. Pharmacol. Exp. Ther.201033437107191:CAS:528:DC%2BC3cXhtFyksL7K10.1124/jpet.110.16727020519553 Manual for Preclinical Studies of New Pharmacological Substances. Part I, Mironov AN, ed. Moscow, 2012. Russian. KuryshevaNICarbonic anhydrase inhibitors in the treatment of glaucomaReview. Part II. Oftalmologiya.202017467668210.18008/1816-5095-2020-4-676-682 Kurysheva NI. Carbonic anhydrase inhibitors in the treatment of glaucoma. Review. Part I. Oftalmologiya. 2020;17(S3):542-549. Russian. doi: https://doi.org/10.18008/1816-5095-2020-3S-542-549 SupuranCTHow many carbonic anhydrase inhibition mechanisms exist?J. Enzyme Inhib. Med. Chem.20163133453601:CAS:528:DC%2BC2MXhvFGms7bE10.3109/14756366.2015.112200126619898 KrasavinMShetnevABaykovSKalininSNocentiniASharoykoVPoliGTuccinardiTKorsakovMTennikovaTBSupuranCTPyridazinone-substituted benzenesulfonamides display potent inhibition of membrane-bound human carbonic anhydrase IX and promising antiproliferative activity against cancer cell linesEur. J. Med. Chem.20191683013141:CAS:528:DC%2BC1MXktFOktr4%3D10.1016/j.ejmech.2019.02.04430826507 Bate ST, Clark RA. The Design and Statistical Analysis of Animal Experiments. Cambridge, 2014. 5835_CR1 F Carta (5835_CR2) 2012; 22 M Krasavin (5835_CR7) 2019; 168 CT Supuran (5835_CR5) 2018; 28 5835_CR6 5835_CR9 CT Supuran (5835_CR3) 2016; 31 F Cianchi (5835_CR8) 2010; 334 NI Kurysheva (5835_CR4) 2020; 17 5835_CR10 |
| References_xml | – reference: Ghorai S, Pulya S, Ghosh K, Panda P, Ghosh B, Gayen S. Structure-activity relationship of human carbonic anhydrase-II inhibitors: Detailed insight for future development as anti-glaucoma agents. Bioorg. Chem. 2020;95:103557. doi: https://doi.org/10.1016/j.bioorg.2019.103557 – reference: Kurysheva NI. Carbonic anhydrase inhibitors in the treatment of glaucoma. Review. Part I. Oftalmologiya. 2020;17(S3):542-549. Russian. doi: https://doi.org/10.18008/1816-5095-2020-3S-542-549 – reference: CianchiFVinciMCSupuranCTPeruzziBDe GiuliPFasolisGPerigliGPastorekovaSPapucciLPiniAMasiniEPuccettiLSelective inhibition of carbonic anhydrase IX decreases cell proliferation and induces ceramide-mediated apoptosis in human cancer cellsJ. Pharmacol. Exp. Ther.201033437107191:CAS:528:DC%2BC3cXhtFyksL7K10.1124/jpet.110.16727020519553 – reference: SupuranCTApplications of carbonic anhydrases inhibitors in renal and central nervous system diseasesExpert Opin. Ther. Pat.201828107137211:CAS:528:DC%2BC1cXhs1Olt77I10.1080/13543776.2018.151902330175635 – reference: KuryshevaNICarbonic anhydrase inhibitors in the treatment of glaucomaReview. Part II. Oftalmologiya.202017467668210.18008/1816-5095-2020-4-676-682 – reference: Bate ST, Clark RA. The Design and Statistical Analysis of Animal Experiments. Cambridge, 2014. – reference: CartaFSupuranCTScozzafavaANovel therapies for glaucoma: a patent review 2007–2011Expert Opin. Ther. Pat.201222179881:CAS:528:DC%2BC38Xjs1Cqug%3D%3D10.1517/13543776.2012.64900622191414 – reference: KrasavinMShetnevABaykovSKalininSNocentiniASharoykoVPoliGTuccinardiTKorsakovMTennikovaTBSupuranCTPyridazinone-substituted benzenesulfonamides display potent inhibition of membrane-bound human carbonic anhydrase IX and promising antiproliferative activity against cancer cell linesEur. J. Med. Chem.20191683013141:CAS:528:DC%2BC1MXktFOktr4%3D10.1016/j.ejmech.2019.02.04430826507 – reference: SupuranCTHow many carbonic anhydrase inhibition mechanisms exist?J. Enzyme Inhib. Med. Chem.20163133453601:CAS:528:DC%2BC2MXhvFGms7bE10.3109/14756366.2015.112200126619898 – reference: Manual for Preclinical Studies of New Pharmacological Substances. Part I, Mironov AN, ed. Moscow, 2012. Russian. – volume: 31 start-page: 345 issue: 3 year: 2016 ident: 5835_CR3 publication-title: J. Enzyme Inhib. Med. Chem. doi: 10.3109/14756366.2015.1122001 – volume: 17 start-page: 676 issue: 4 year: 2020 ident: 5835_CR4 publication-title: Review. Part II. Oftalmologiya. doi: 10.18008/1816-5095-2020-4-676-682 – volume: 22 start-page: 79 issue: 1 year: 2012 ident: 5835_CR2 publication-title: Expert Opin. Ther. Pat. doi: 10.1517/13543776.2012.649006 – volume: 28 start-page: 713 issue: 10 year: 2018 ident: 5835_CR5 publication-title: Expert Opin. Ther. Pat. doi: 10.1080/13543776.2018.1519023 – ident: 5835_CR1 doi: 10.18008/1816-5095-2020-3S-542-549 – ident: 5835_CR6 doi: 10.1016/j.bioorg.2019.103557 – ident: 5835_CR10 doi: 10.1017/CBO9781139344319 – volume: 168 start-page: 301 year: 2019 ident: 5835_CR7 publication-title: Eur. J. Med. Chem. doi: 10.1016/j.ejmech.2019.02.044 – volume: 334 start-page: 710 issue: 3 year: 2010 ident: 5835_CR8 publication-title: J. Pharmacol. Exp. Ther. doi: 10.1124/jpet.110.167270 – ident: 5835_CR9 |
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| SubjectTerms | Acute toxicity Analysis Animals Antibiotics Antidepressants Antigens, Neoplasm Biomedical and Life Sciences Biomedicine Brinzolamide Carbon dioxide Carbonic Anhydrase Inhibitors - pharmacology Carbonic anhydrases Carbonic Anhydrases - metabolism Cell Biology Drugs Enzymes Glaucoma Internal Medicine Isoforms Laboratory animals Laboratory Medicine Medical practices Pathology Pedagogy Pharmaceuticals Physiology Protein Isoforms Rabbits Respiration Structure-Activity Relationship Sulfonamides Sulfonamides - pharmacology Toxicology |
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| Title | Pharmacological Properties of Sulfonamide Derivatives, New Inhibitors of Carbonic Anhydrase |
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